Does MIRABEGRON Cause Intentional product misuse? 1,416 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,416 reports of Intentional product misuse have been filed in association with MIRABEGRON (MIRABEGRON). This represents 6.9% of all adverse event reports for MIRABEGRON.
1,416
Reports of Intentional product misuse with MIRABEGRON
6.9%
of all MIRABEGRON reports
18
Deaths
62
Hospitalizations
How Dangerous Is Intentional product misuse From MIRABEGRON?
Of the 1,416 reports, 18 (1.3%) resulted in death, 62 (4.4%) required hospitalization, and 15 (1.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIRABEGRON. However, 1,416 reports have been filed with the FAERS database.
What Other Side Effects Does MIRABEGRON Cause?
Drug ineffective (4,151)
Off label use (1,704)
Dizziness (1,297)
Headache (1,288)
Blood pressure increased (1,100)
Hypertension (1,057)
Dry mouth (1,034)
Diarrhoea (921)
Pain (921)
Intentional product use issue (917)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which MIRABEGRON Alternatives Have Lower Intentional product misuse Risk?
MIRABEGRON vs MIRALAX
MIRABEGRON vs MIRCERA
MIRABEGRON vs MIRENA
MIRABEGRON vs MIRIKIZUMAB-MRKZ
MIRABEGRON vs MIRTAZAPINE